Comparing Viral Vectors and Fate Mapping Approaches for Astrocyte-to-Neuron Reprogramming in the Injured Mouse Cerebral Cortex

Cells. 2024 Aug 23;13(17):1408. doi: 10.3390/cells13171408.

Abstract

Direct neuronal reprogramming is a promising approach to replace neurons lost due to disease via the conversion of endogenous glia reacting to brain injury into neurons. However, it is essential to demonstrate that the newly generated neurons originate from glial cells and/or show that they are not pre-existing endogenous neurons. Here, we use controls for both requirements while comparing two viral vector systems (Mo-MLVs and AAVs) for the expression of the same neurogenic factor, the phosphorylation-resistant form of Neurogenin2. Our results show that Mo-MLVs targeting proliferating glial cells after traumatic brain injury reliably convert astrocytes into neurons, as assessed by genetic fate mapping of astrocytes. Conversely, expressing the same neurogenic factor in a flexed AAV system results in artefactual labelling of endogenous neurons fatemapped by birthdating in development that are negative for the genetic fate mapping marker induced in astrocytes. These results are further corroborated by chronic live in vivo imaging. Taken together, the phosphorylation-resistant form of Neurogenin2 is more efficient in reprogramming reactive glia into neurons than its wildtype counterpart in vivo using retroviral vectors (Mo-MLVs) targeting proliferating glia. Conversely, AAV-mediated expression generates artefacts and is not sufficient to achieve fate conversion.

Keywords: AAV; Neurogenin2; astrocytes; birthdating; direct reprogramming; fate mapping; neurons; retrovirus; viral vectors.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Astrocytes* / metabolism
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Cellular Reprogramming* / genetics
  • Cerebral Cortex* / metabolism
  • Cerebral Cortex* / pathology
  • Dependovirus* / genetics
  • Genetic Vectors* / genetics
  • Genetic Vectors* / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Neurons* / metabolism
  • Retroviridae / genetics

Substances

  • Nerve Tissue Proteins
  • Basic Helix-Loop-Helix Transcription Factors
  • Neurog2 protein, mouse